State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Peking Union Medical College & Chinese Academy of Medical Sciences, Beijing 100050, China.
J Chromatogr A. 2013 Aug 23;1304:257-62. doi: 10.1016/j.chroma.2013.07.008. Epub 2013 Jul 5.
The use of two-dimensional liquid chromatography (2D-LC) for quantification studies presents challenges with respect to repeatability, precision, and robustness. The present study used an on-line stop-flow heart-cutting 2D-LC system to determine 12 chemical constituents in tartary buckwheat. A combination of various stationary phases was developed and bridged using two switch valves as the interface. Hydrophilic interaction chromatography was chosen for separation in the first dimension ((1)D), and mixed mode stationary phases (an amide polar-embedded phase and alkyl-phenyl phase) were used in parallel for separation in the second dimension ((2)D). The mobile phase comprised acetonitrile and water containing 0.03% aqueous phosphoric acid. The sample was separated into two fractions on the (1)D column (HILIC-10 column) using 5% acetonitrile. One fraction, mainly comprising flavonoids, was directly eluted onto the head of (2)D column (Polar Advantage II column) and further separated using a linear gradient of 11-23% acetonitrile. The second fraction, containing phenylpropanoid glycosides, was trapped on the (1)D column. This retained fraction was back-flushed onto the (2)D column (Phenyl-1 column) and separated using a linear gradient of 35-43% acetonitrile. An on-line stop-flow heart-cutting 2D-LC system was successfully developed with column switching and back-flush. This 2D-LC system was validated and was able to simultaneously determine 12 major components in tartary buckwheat: seven flavonoids, four phenylpropanoid glycosides, and N-trans-feruloyltyramine. The system showed good performance with respect to linearity (r>0.996), repeatability (RSD, relative standard deviation<3.4%), intra-day and inter-day precision (RSD<4.6%), recovery (91.2-108%), limit of detection (LOD) (0.05-0.21μg/mL), and limit of quantification (LOQ) (0.10-0.41μg/mL). The on-line stop-flow heart-cutting 2D-LC system offers a potential approach to analyze compounds, which have similar structures but different polarities, in herbal medicines.
二维液相色谱(2D-LC)用于定量研究存在可重复性、精密度和稳健性方面的挑战。本研究采用在线停流心切割 2D-LC 系统测定苦荞中的 12 种化学成分。开发了各种固定相的组合,并使用两个切换阀作为接口桥接。亲水作用色谱法(HILIC)用于一维(1D)分离,混合模式固定相(酰胺极性嵌入相和烷基-苯基相)用于二维(2D)分离。流动相由含 0.03%磷酸的乙腈和水组成。样品在 1D 柱(HILIC-10 柱)上分离成两部分,用 5%乙腈洗脱。一部分主要包含黄酮类化合物,直接洗脱到 2D 柱(Polar Advantage II 柱)的头部,并进一步用 11-23%乙腈线性梯度洗脱。第二部分,含有苯丙素糖苷,被保留在 1D 柱上。该保留部分被反冲洗到 2D 柱(Phenyl-1 柱)上,并使用 35-43%乙腈的线性梯度洗脱。成功开发了带有柱切换和反冲洗的在线停流心切割 2D-LC 系统。该 2D-LC 系统经过验证,能够同时测定苦荞中的 12 种主要成分:7 种黄酮类化合物、4 种苯丙素糖苷和 N-反式-阿魏酰酪胺。该系统在线性(r>0.996)、重复性(RSD,相对标准偏差<3.4%)、日内和日间精密度(RSD<4.6%)、回收率(91.2-108%)、检测限(LOD)(0.05-0.21μg/mL)和定量限(LOQ)(0.10-0.41μg/mL)方面表现良好。在线停流心切割 2D-LC 系统为分析中草药中具有相似结构但极性不同的化合物提供了一种潜在的方法。